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Completed Phase 4 Interventional

Study To Evaluate The Efficacy And Safety Of Ciprofloxacin Extended-Release (Cipro® XR) 1000 mg Tablets Given Once Daily For 7 To 14 Days In The Treatment Of Patients 18 Years Or Older With Complicated Urinary Tract Infections Caused By Pseudomonas Aeruginosa And Other Common Uropathogens

ClinicalTrials.gov ID: NCT00481689

Public ClinicalTrials.gov record NCT00481689. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 5:27 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Prospective, Open-Label, Noncomparative, Multicenter Study to Evaluate the Efficacy and Safety of Ciprofloxacin Extended Release (Cipro XR) 1000 mg Tablets Given Once Daily for 7 to 14 Days in the Treatment of Patients 18 Years or Older With Complicated Urinary Tract Infections Caused by Pseudomonas Aeruginosa and Other Common Uropathogens

Study identification

NCT ID
NCT00481689
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Bayer
Industry
Enrollment
500 participants

Conditions and interventions

Interventions

  • Cipro XR (Ciprofloxacin, BAYQ3939) Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2004
Primary completion
Not listed
Completion
Aug 31, 2005
Last update posted
Jun 25, 2009

2004 – 2005

United States locations

U.S. sites
35
U.S. states
20
U.S. cities
33
Facility City State ZIP Site status
Not listed Birmingham Alabama 35206
Not listed Birmingham Alabama 35209
Not listed Huntsville Alabama 35801
Not listed Scottsdale Arizona 85258
Not listed Cudahy California 90201
Not listed Fresno California 93720-0153
Not listed La Mesa California 91942-3058
Not listed Laguna Hills California 92653
Not listed Long Beach California 90806
Not listed Los Angeles California 90015
Not listed San Diego California 92103
Not listed Torrance California 90503
Not listed Waterbury Connecticut 06708
Not listed Ocala Florida 34474
Not listed Pembroke Pines Florida 33027
Not listed Indianapolis Indiana 46202
Not listed Des Moines Iowa 50309
Not listed Iowa City Iowa 52242-1089
Not listed Watertown Massachusetts 02472
Not listed St Louis Missouri 63125
Not listed Las Vegas Nevada 89109
Not listed Reno Nevada 89511-2069
Not listed East Orange New Jersey 07918
Not listed Albuquerque New Mexico 87102
Not listed Albuquerque New Mexico 87109
Not listed Manhasset New York 11030-1961
Not listed North Massapequa New York 11758
Not listed Troy New York 12180-1695
Not listed Eugene Oregon 97401
Not listed Philadelphia Pennsylvania 19107-5096
Not listed Memphis Tennessee 38119
Not listed San Antonio Texas 78229
Not listed Richmond Virginia 23249-0002
Not listed Tacoma Washington 98431-5000
Not listed Cheyenne Wyoming 82001

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00481689, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 25, 2009 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00481689 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →